Prospective PRO/QoL Registry for Patients With Bone Metastases of Breast or Prostate Cancer (PROBone)
Status
Conditions
Details and patient eligibility
About
Evaluation of patient reported outcomes (PRO) / QoL regarding typical ailments in real-life patients with bone metastases treated with osteoprotective agents.
Full description
The PRO Bone project will recruit a representative cohort of patients with breast or prostate cancer suffering from bone metastases. The aim of this study is to collect data on Patient Reported Outcomes (PRO)/Quality of Life regarding bone pain and the impact of bone pain on quality of life and daily activities. PROs are assessed by a questionnaire consisting of a visual analog scale for bone pain, two questions regarding bone pain management, the bone pain module of FACT questionnaire (FACT-BP) and four questions addressing the impact of treatment on daily life (overall, social life, ability to work and ability to perform routine tasks)
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Histologically confirmed metastatic breast or prostate cancer
- Start of first systemic osteoprotective treatment
- Ability to read and understand German
- Written informed consent
Exclusion criteria
• None
Trial contacts and locations
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal